Clinical Data Coordinator II (CDC II)
Job Locations: India – Chennai | Bangalore | Trivandrum
Work Model: Office with Flex (Hybrid)
Employment Type: Full-Time
Experience Required: 4–6 Years
Job Requisition ID: JR141730
Industry: Clinical Research | Clinical Data Management | CRO
About ICON plc
ICON plc is a global leader in healthcare intelligence and clinical research, supporting the development of innovative therapies that improve patient outcomes worldwide. With a strong focus on quality, regulatory compliance, and data-driven clinical development, ICON partners with pharmaceutical, biotechnology, and medical device companies across all phases of clinical trials.
Role Overview
The Clinical Data Coordinator II (CDC II) supports end-to-end clinical data management activities for global clinical studies. This role works closely with Clinical Data Scientists and Study Leads to ensure accurate, complete, and timely clinical trial data. The position requires hands-on experience in eCRF maintenance, data reconciliation, and issue resolution within regulated clinical research environments.
Key Responsibilities
Support the Data Management Study Lead in maintaining eCRFs, Data Validation Specifications, and study-specific procedures
Perform reconciliation of clinical and third-party data in accordance with edit check specifications and data review plans
Track, analyze, and communicate study-level data metrics and task status to Clinical Data Scientists, project teams, and functional management
Address data-related queries and recommend effective solutions to data issues
Perform root cause analysis to identify and resolve recurring data discrepancies
Ensure compliance with internal SOPs, study protocols, and regulatory requirements
Collaborate with cross-functional teams to support high-quality data delivery
Required Qualifications
Bachelor’s degree in Life Sciences, Healthcare, Pharmacy, or a related discipline
4–6 years of relevant experience in clinical data management within a CRO, pharmaceutical, or biotechnology organization
Working knowledge of clinical data management processes and lifecycle activities
Experience using clinical data management systems such as Medidata Rave, Oracle RDC, or equivalent platforms
Strong attention to detail with the ability to manage multiple priorities in a fast-paced environment
Effective written and verbal communication skills
Ability to collaborate across global and cross-functional teams
Preferred Skills
Knowledge of ICH-GCP guidelines and regulatory standards
Experience supporting Phase I–IV clinical trials
Familiarity with third-party data sources and reconciliation processes
Work Environment and Benefits
ICON offers a flexible hybrid work model supported by competitive compensation and comprehensive benefits. These include health insurance options, retirement planning, paid leave programs, employee wellness initiatives, and access to global employee assistance resources.
Diversity and Equal Opportunity
ICON is committed to fostering an inclusive and diverse workplace. All qualified applicants will receive equal consideration for employment without discrimination based on race, gender, disability, age, or any other protected status.
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